Canonical Allele Identifier: PA658809385
Gene: TTN HGNC NCBI

Linked Data

ClinVar Variation Id: 46967

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003310.4:p.Asp5408His
CA139661
NM_003319.4:c.16222G>C